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"Adnes" Ultron artificial electronic ear - Taiwan Registration 5df0cfe0f900a231205b72acdaf7c9db

Access comprehensive regulatory information for "Adnes" Ultron artificial electronic ear in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5df0cfe0f900a231205b72acdaf7c9db and manufactured by Advanced Bionics, LLC. The authorized representative in Taiwan is I-LISTEN BIOTECHNOLOGICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ADVANCED BIONICS, LLC, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5df0cfe0f900a231205b72acdaf7c9db
Registration Details
Taiwan FDA Registration: 5df0cfe0f900a231205b72acdaf7c9db
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Device Details

"Adnes" Ultron artificial electronic ear
TW: โ€œ่‰พๅพทๅฐผๆ–ฏโ€ๅฅงๅ‰ตไบบๅทฅ้›ปๅญ่€ณ
Risk Class 3

Registration Details

5df0cfe0f900a231205b72acdaf7c9db

DHA05603167607

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT Science

G.0001 Artificial ear bug implanter

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input

Dates and Status

Oct 12, 2018

Oct 12, 2028

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